Year-end Sale % OFF 
Abstract
Using 1,2-Acenaphthenedione as an example, cyclic voltammetry, chronoamperometry, coulometry, electrolysis and digital simulation were used to show that electroreduction of carbonyl compounds in the presence of nitromethane in 0.1 M Bu4NClO4/DMF proceeds via the ECE mechanism gives rise nitromethane anion initiating cyclic nitroaldol (Henry) process leading to β-nitroalcohols.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
